Site Engagement Liaison
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring recent medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Site Engagement Liaison at ICON, you will foster relationships with clinical trial sites, enhancing site engagement, and contribute to the advancement of cutting-edge treatments and therapies.

What You Will Do:

You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:
Building and maintaining robust relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff.
Providing support and guidance to site staff on study protocols, procedures, and regulatory requirements, ensuring compliance and successful study conduct.




Identifying opportunities to improve site engagement and optimize site performance through regular communication and feedback mechanisms.
Collaborating with internal teams to develop and implement site engagement strategies tailored to the specific needs of each study and site.
Monitoring site performance metrics and providing regular updates to study teams on site engagement activities and outcomes.

Your Profile:

Required qualifications and experience:
Bachelor's/ Master's degree in life sciences or a related field.
Previous experience in clinical research, site management, or a related field preferred. (i.e. right from Pre-Trials Assessment to Close outs)
Min. 2 years experience in Project Management or Clinical Trial Management in an MNC
Min 8+ years in Onsite monitoring experience with 5+ years in MNC
Should be responsible for complete Site Management
Should have SEC (Subject Expert Committee) presentati

📌 Site Engagement Liaison Bengaluru
🏢 IRE
📍 Bengaluru